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| 1 | Salt formation to improve drug solubility显示文摘 | Serajuddin AT | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 2 | Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems and recent breakthroughs显示文摘 | Serajuddin AT | 1999 | J Pharm Sci1999，88，10： | 1 |
| 3 | Solid dispersion of poorly water soluble drugs: early promises, subsequent problems, and recent breakthroughs 显示文摘 | SERAJUDDIN AT | 1999 | J Pharm Sci1999，88，10： | 1 |
| 4 | Relative lipophilicities, solubilities, and structure pharmacological considerations of 3-hydroxy-3 -methylglutaryl-coenzyme Areduetase inhibitors pravastatin, lovastatin, mevastatin, and simvastatin显示文摘 | Serajuddin AT Ranadive SA Mahoney EM | 1991 | J Pharm Sei1991，80，9： | 1 |
| 5 | Salt formation to improve drug solubility 显示文摘 | Serajuddin AT | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 6 | Solid dispersion of poorly water mluble drugs early promises, subsequent problems and recent breakthroughs 显示文摘 | Serajuddin AT | 1999 | J Pharm Sei1999，88，10： | 1 |
| 7 | Selection of solid dosage form composition through drug excipient com- patibility testing 显示文摘 | Serajuddin AT Thakur AB Ghoshal RN | 1999 | Journal of Pharmaceutical Sciences 1999 American Chemical Society1999，30，7： | 1 |
| 8 | Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent break- throughs显示文摘 | Serajuddin AT | 1999 | J Pharm Sci1999，88，1： | 1 |
| 9 | Salt formation to improve drug solubility显示文摘 | Serajuddin AT | 2007 | Adv Drug Deliv Rev2007，59，7： | 1 |
| 10 | Improved dissolution of a poorly water soluble drug from solid dispersions in PEG:polysorbate 80显示文摘 | Serajuddin AT Sheen PC AugustineMA | 1990 | J Pharm Sci1990，79，5： | 1 |
| 11 | Solid dispersion of poorly water-soluble drugs:early promises,subsequent problems and recent breakthroughs显示文摘 | SERAJUDDIN AT | 1999 | J Pharm Sci1999，88，10： | 1 |
| 12 | Selection of solid dosage from composition through drug-excipient compatibility testing显示文摘 | Serajuddin AT Thakur AB Ghoshal RN | 1999 | Pharm Sci1999，88，7： | 1 |
| 13 | Relative lipophilicities,solubiliies,and structure-pharmacoloaical considerations of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors pravastatin,lovastatin,mevastatin,and simvastatin显示文摘 | Serajuddin AT Ranadive SA Mahoney EM | 1991 | J Pharm Sci1991，80，9： | 1 |
| 14 | Common ion effect on solubility and dissolution rate of the sodium salt of an organic acid显示文摘 | Serajuddin AT Sheen PC Augustine MA | | 0，，8： | 1 |
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